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Enseal NSEAL514RHRecalls & reported problems

Ethicon Endo-Surgery, LLC · Enseal Temperature Controlled Tissue Sealing Technology Disposable Tissue Sealing Device Taptronic Trigger Activated Power 5mm Jaw Style · Class 2

All models of Enseal (24)

Data updated Oct 16, 2026 from official FDA records · Editorial policy

Adverse event reports
1
Deaths reported
0
Injuries reported
0
Recalls naming it
0

Summary

The FDA's MAUDE database contains 1 adverse event report that list this exact device (DI 10705036000020), received between Sep 9, 2022 and Sep 9, 2022 — classified as 1 malfunction.

The most frequently reported specific device problem is “Difficult to Open or Close” (1 report).

Reports come from manufacturers, hospitals and patients and are not verified by the FDA. A report does not prove the device caused the event, and counts can't be used to compare devices or estimate failure rates. What reports can and can't tell you · How this data works · Data updated Oct 16, 2026.

Most reported problems

Device problems

  • Difficult to Open or Close1
  • Material Integrity Problem1

Patient problems

  • No Clinical Signs, Symptoms or Conditions1

Recent adverse event reports

The 1 most recent of 1 reports, in the reporter's own words as published by the FDA.

  • MalfunctionSep 9, 2022Difficult to Open or Close; Material Integrity Problem; Difficult to Open or Close; Material Integrity Problem

    IT WAS REPORTED THAT DURING A VET PROCEDURE: OOPHORECTOMY THE JAWS DID NOT OPEN PROPERLY AND BLADE WAS MISALIGNED. NO AE. DEVICE REPLACED. PROCEDURE COMPLETED WITH MANUAL SUTURE.

    Patient problems: No Clinical Signs, Symptoms or Conditions

    MAUDE report 15391985 ↗

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Sources and updates

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